Tag | Content |
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EnhancerAtlas ID | HS146-04435 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr14:24820640-24821790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr14:24821281-24821294 | TGAATTTGCATGT | + | 6.05 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr14 | 24821274 | 24821506 | chr14 | 24821586 | 24821671 | chr14 | 24820749 | 24821093 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I024351 | chr14 | 24820641 | 24821108 |
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Enhancer Sequence | ACAAAGCTAC AAGGAGCTGT GATCCCACCA CTGCACTCCA GCCTGGGTGG CAGAGTGAGA 60 CCCTGTCTAA TAAAAGAAAA GAAAATGTAA CTTTGGCGTT CTTTGGCTGG AGTTTGGTGC 120 TATCTGTGGT TTCAGGTCTC CACTAGGGGT CTTGGAACAT ATCCCCACAG ATAAGGGGGA 180 ATATCGTATC TCTCTTTTGC CAGCTGGCAT AGTGTTAAGC GCTGTCAGTA GTGGGTGCTG 240 GAGGAACACT GGAGCAGGAA GAAGTCCATC TTCCTGGTTT TGGTTTGCTC CTTTGCCTTA 300 CTCCTGCAGC GTGTGCAATT TCTTCAGTGT ACACTCAGGC AGTGCAAAGT GGTCAGCAGT 360 GCCTAGCAGC CAAAAGCTTC CCCTGGCACA TTTCTGGGTG ACTTCTCAGC CTGTTGCAAC 420 TGCTAAGGCA CCTCCCCATG AATAACTTGC TTTGGCATCT GCTTGGCCAA TTTCACAGCT 480 ATTTCAGCCC TAGGAGTAGT GGGTTTTTCT TAAATTTGCT GTTCCTGTGT CCTTTGGAAT 540 TCTCATTTCT TCTTACTAGC TAATCCCTTA GTATGCCAAC ACCCTGTTGG AGTTAATGCT 600 TCTTTATTTT ATTTTTGCAA ATAAAAATAT GAGACACTCC ATGAATTTGC ATGTCATCCT 660 TGTGCAGGGG CCATCCTATT CTTCTCTGTA TCATTTTAGT ATATGTGTTG CCAAAGTGAG 720 CACAATACTT GTTTATATTA AACGTTCCTG TTTCAAATGA CTGTGTGGTT TCTGTGTCCT 780 GATTAAACCC TGACCGATAC AGCTTTAGTC CTAGAATATA GTTCTTCAGG GACGCTAACG 840 ATATCCTGTG GTGTTTAACA GGTCCTTCCT CCTTAACAGG TCCTAAATTC CCATTTTTGT 900 TTTCTCAGGA CTGTAGACTA CTGAAAGTTC TTCTCAGCCT CCTACCTCTT AGGCACTATC 960 TCCTGCTGAG TCTGGCTGCC TCTCACAAAT CGATAAATAT CCCCCATGGG ACAGACCATG 1020 CAGAATGTTG GCCTCACCTC AACATGCTTT CCCTTTCTTC TGGGACGTTG GCCCTTCAAA 1080 GCCTCCTGCC TTGATGAATT TCCACTGTCT TCAAACATAT TTAAAAAAAT TTGTACCCAG 1140 CTATGCAAAG 1150
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